Hemophagocytic Syndrome in a Patient with Adult-onset Still's Disease
Yükleniyor...
Dosyalar
Tarih
2011
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Turkish League Against Rheumatism
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Hemophagocytic syndrome is a fatal and life-threatening syndrome characterized by pancytopenia and multiple organ failure. It can frequently be seen in childhood as a primary or familial condition. In adults, it occurs secondarily. In etiology, wide range of factors are related to this syndrome. Adult-onset Still's disease seems to be one of the systemic rheumatological diseases that cause this syndrome. In our literature review, we found few studies related to this syndrome. In this article, we report a 40-year-old female patient who had been treated with the diagnosis of Adult-onset Still's disease for four years in our clinic and who developed hemophagocytic syndrome during her follow-ups.
Açıklama
WOS: 000295972800009
Anahtar Kelimeler
Adult-onset still's disease, hemophagocytic syndrome, hemophagocytosis
Kaynak
Turkish Journal Of Rheumatology
WoS Q Değeri
Q4
Scopus Q Değeri
N/A
Cilt
26
Sayı
2
